rs17597926
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs17597926(A;A) |
Make rs17597926(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 55538707 |
Gene | TCF4 |
is a | snp |
is | mentioned by |
dbSNP | rs17597926 |
dbSNP (classic) | rs17597926 |
ClinGen | rs17597926 |
ebi | rs17597926 |
HLI | rs17597926 |
Exac | rs17597926 |
Gnomad | rs17597926 |
Varsome | rs17597926 |
LitVar | rs17597926 |
Map | rs17597926 |
PheGenI | rs17597926 |
Biobank | rs17597926 |
1000 genomes | rs17597926 |
hgdp | rs17597926 |
ensembl | rs17597926 |
geneview | rs17597926 |
scholar | rs17597926 |
rs17597926 | |
pharmgkb | rs17597926 |
gwascentral | rs17597926 |
openSNP | rs17597926 |
23andMe | rs17597926 |
SNPshot | rs17597926 |
SNPdbe | rs17597926 |
MSV3d | rs17597926 |
GWAS Ctlg | rs17597926 |
GMAF | 0.01377 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22451930] Schizophrenia risk polymorphisms in the TCF4 gene interact with smoking in the modulation of auditory sensory gating
GWAS snp | |
---|---|
PMID | [PMID 22688191![]() |
Trait | |
Title | Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder. |
Risk Allele | |
P-val | 1E-7 |
Odds Ratio | 1.3600 None |